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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 256-269 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A time-dependent adiabatic electronic representation is defined by solving the local N-level electronic time-dependent Schrödinger equations at each nuclear configuration of a general N-channel, laser-driven molecular system. These solutions are eigenstates of a time-dependent effective Hamiltonian with respect to which the exact time-evolution of the N-state system is adiabatic. For a two-channel system, the time-dependent adiabatic electronic representation depends on an effective area of the laser pulse and geometrical phases that are also functionals of the laser pulse shape. This adiabatic representation is used in constructing an algorithm for the generation and propagation of wavepackets in a two-channel system irradiated by a short laser pulse. The algorithm is applied to the study of the wavepacket dynamics in the Na–Ar collisional system excited by short laser pulses. The dynamics of the channel populations are analyzed as functions of the shape, duration, and intensity of the laser pulses.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 5497-5515 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The wave packet dynamics of the photodissociation of H2+ under excitation by laser pulses of short durations at 329.7 nm are studied. The photodissociation process involves essentially two coupled channels, and the detailed mechanism for the formation of fragment kinetic energy spectra is examined by following the evolution of structures in the coupled-channel wave functions in momentum space. These structures appear in the channels' momentum wave functions at P≠0, as the v=0 ground vibrational state is promoted to the dissociative channel then accelerated. The variations of these structures reflect the interplay between local laser-induced transitions and the accelerating–decelerating action of intrinsic molecular forces. The wave packet dynamics are studied for rectangular and Gaussian pulses of varying durations and peak intensities. In addition, two forms of channel couplings were considered corresponding to two different choices of the gauge: the electric-field (EF) gauge, in which the matter–field interaction is of the length form and the radiation-field (RF) gauge, in which it is of the velocity form.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1941-1950 
    ISSN: 0887-6266
    Keywords: rigid-rod polymer ; cation ; dialysis ; molecular weight ; cast ; aggregated ; isotropic ; anisotropic ; film ; depletion measurement ; ionic conductivity ; x-ray scattering ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly[(1,7-dihydrobenzo[1,2-d:4,5-d′] diimidazole-2,6-diyl)-2-(2-sulfo)-p-phenylene], a conjugated rigid-rod polymer, was derivatized with pendants of propane-sulfonated ionomers. The derivatized rigid-rod polymer was soluble in aprotic solvents as well as in water for isotropic solutions that were processed into isotropic films. Direct-current electrical conductivity σ of the films was measured using the four-probe technique. Room-temperature σ as high as 2.9 × 10-4S/cm was achieved on pristine isotropic films without using dopants. When the rigid-rod polymer concentration exceeded 25 wt %, the isotropic solution could be transformed into a liquid-crystalline solution that allowed deformations to be applied to produce anisotropic films. Significant increase in σ was obtained in a sheared film along both the parallel direction (∥) and the transverse direction (⊥) with a σ∥/σ⊥ = 5. Additionally, enhanced σ was realized in films heat-treated at about 100°C, in the derivatized polymer with higher molecular weight from dialysis, and in substituting the sulfonated ion Na+ by H+ in the pendants of the polymers. Constant-voltage measurements were applied to the polymers to monitor the σ stability for ascertaining the nature of the conductivity. No electronic contribution in σ was detected. Instead, a monotonically decreasing σ was consistently observed indicative of ionic conductivity. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    International Journal for Numerical Methods in Fluids 16 (1993), S. 777-791 
    ISSN: 0271-2091
    Keywords: Vortex sheet ; Propeller slipstream ; Propeller-airframe integration ; Finite volume ; Full potential ; Transonic flow ; Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: This paper summarizes a combined analytical-computational technique which models vortex sheets in transonic potential-flow methods. In this approach, the inviscid nature of discontinuities across vortex sheets is preserved by employing the step function to remove singularities at these surfaces. The location and strength of the vortex sheets are determined by satisfying the flow-tangency boundary condition and the vorticity transport equation. The theory is formulated for the general three-dimensional case, but its application is confined to the problem of computing slipstreams behind propellers with free-vortex blading in axisymmetric flows.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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